ID

30191

Description

Study ID: 102123 Clinical Study ID: FFR102123 Study Title: A randomised double-blind placebo controlled parallel group multicentre long term study to evaluate the safety of once-daily, intranasal administration of GW685698X aqueous nasal spray 100mcg* for 52 weeks in adult and adolescent subjects with perennial allergic rhinitis. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: FLUTIDE, Allermist, Veramyst, FLUNASE, FLIXOTAIDE, FLUTAIDE, FLIXOVATE, Avamys; Veramyst, Avamys, Allermist Study Indication: Rhinitis, Allergic, Perennial This ODM-file contains Administrative Data (Visit 1).

Mots-clés

  1. 18/05/2018 18/05/2018 - Sarah Riepenhausen
Détendeur de droits

GlaxoSmithKline

Téléchargé le

18 mai 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Safety of once-daily administration of Fluticasone nasal spray in adults and adolescents with perennial allergic rhinitis GSK 102123

Administrative Data - Visit 1

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject identifier
Description

Subject identifier

Type de données

text

Alias
UMLS CUI [1]
C2348585
Centre Number
Description

Centre Number

Type de données

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Visit Date
Description

Visit Date

Type de données

date

Alias
UMLS CUI [1]
C1320303
Demography
Description

Demography

Alias
UMLS CUI-1
C0011298
Date of Birth
Description

Date of Birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Gender

Type de données

text

Alias
UMLS CUI [1]
C0079399
Pick the racial group which best describes the subject’s racial origin.
Description

The racial groups below are based on the subject’s genotypical racial origin, not nationality or where they currently reside. American Hispanic: With racial origin in Central or South America Arabic/North African: With racial origin in North Africa/Middle East Black: With racial origin in Central, East or West Africa East and South East Asian: With racial origin in East and South East Asia, e.g., Chinese, Korean, Thai, Vietnamese Japanese: With racial origin in Japan South Asian: With racial origin in South Asia e.g., Indian, Pakistani White/Caucasian: With racial origin in Europe Other: With racial origin not represented above or whose predominate origin can not be determined

Type de données

text

Alias
UMLS CUI [1]
C0034510
Screen Failure
Description

Screen Failure

Alias
UMLS CUI-1
C1710476
Was this subject a screen failure?
Description

A subject who is assigned a subject number, but is not randomised has failed screening.

Type de données

text

Alias
UMLS CUI [1]
C1710476
Screen Failure Date
Description

Screen Failure Date

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1710476
If screen failure, what was the primary reason?
Description

If adverse event, record details in the Non-Serious Adverse Events or Serious Adverse Event forms as appropriate.

Type de données

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0392360
If other reason for screen failure, specify:
Description

Other Reason for Screen Failure

Type de données

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0392360

Similar models

Administrative Data - Visit 1

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject identifier
Item
Subject identifier
text
C2348585 (UMLS CUI [1])
Centre Number
Item
Centre Number
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item Group
Demography
C0011298 (UMLS CUI-1)
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Code List
Sex
CL Item
Male (M)
CL Item
Female (F)
Item
Pick the racial group which best describes the subject’s racial origin.
text
C0034510 (UMLS CUI [1])
Code List
Pick the racial group which best describes the subject’s racial origin.
CL Item
American Hispanic (1)
CL Item
Arabic/North African (2)
CL Item
Black (3)
CL Item
East and South East Asian (4)
CL Item
Japanese (5)
CL Item
South Asian (6)
CL Item
White/Caucasian (7)
CL Item
Other (Z)
Item Group
Screen Failure
C1710476 (UMLS CUI-1)
Item
Was this subject a screen failure?
text
C1710476 (UMLS CUI [1])
Code List
Was this subject a screen failure?
CL Item
Yes (Y)
CL Item
No (N)
Screen Failure Date
Item
Screen Failure Date
date
C0011008 (UMLS CUI [1,1])
C1710476 (UMLS CUI [1,2])
Item
If screen failure, what was the primary reason?
text
C1710476 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
If screen failure, what was the primary reason?
CL Item
Adverse Event (1)
CL Item
Lost to follow-up (2)
CL Item
protocol violation (3)
CL Item
Subject decided to withdraw from study (4)
CL Item
Did not fulfill eligibility criteria (6)
CL Item
Other (OT)
Other Reason for Screen Failure
Item
If other reason for screen failure, specify:
text
C1710476 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial